Stake attention in this memory
chemical reaction
mechanism
organic chemistry
deprotonation
synthesis
The image depicts an organic chemistry reaction mechanism. It begins with a cyclic ketone undergoing deprotonation at the alpha-carbon using a base, followed by alkylation with methyl iodide (MeI) to add a methyl group. The reaction is repeated with excess potassium hydride (KH) and MeI, adding two more methyl groups. Finally, the ketone undergoes a reaction with sodium amide (NaNH2) in ether (Et2O) to form an allylic double bond. The final product is an unsaturated cyclic ketone.
Loading AttnAds…
transactions
revenues
stakers
Earliest
Latest
Highest stake
No transactions found
